## Create an environment (Currently on OS)
conda create -n nf -c bioconda nextflow -y;
## Due to arm64 architecture, conda environment created with osx-64
CONDA_SUBDIR=osx-64 conda create -n nf -y;
## Install Relevant packages to assignment
conda activate nf;
conda install -c bioconda -c conda-forge entrez-direct sra-tools fastqc trimmomatic skesa spades pigz tree nextflow fastp csvtk -y;
conda install bioconda::seqkit;
conda activate nf
- These sample data were located in the
test_data/folder. - Species: Listeria monocytogenes
- Sample IDs: SRR33049470, SRR33028439
- Nextflow version 24.10.5.5935
- Tools Selected include fastp, skesa, and seqkit
- Fastp was initially ran on raw Fastq sequences. These sequences were downloaded by the commands in
cmds.sh. - After revising and trimming the reads using
nextflow workflow_parallel_sequential.nf --reads "test_data/*_{1,2}.fastq.gz"
